BLUE JAY (UDI BJ240105)
Manufactured by Beijing Choice Electronic Technology Co., Ltd.
Device Regulatory Overview
The BLUE JAY (Model/Catalog Number: BJ240105) is a medical device manufactured by Beijing Choice Electronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification DQA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BJ240105
- Product Code / EMDN
- DQA
- Device Name
- BLUE JAY FINGER PULSE OXIMETER BJ240105
- Database Sync Date
- 2026-08-09 09:11:07
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BLUE JAY?
The registered manufacturer of record for BLUE JAY is Beijing Choice Electronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for BLUE JAY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BJ240105.
What classification code is assigned to this device?
This device is registered under product classification code DQA.
Similar Classification Devices (DQA)
Other Devices by Beijing Choice Electronic Technology Co., Ltd.
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